MolNFT v1 · #129096 · protein
FE(II)/(ALPHA)KETOGLUTARATE-dependent dioxygenase ASQJ_V72I mutant in complex with demethylated cyclopeptin (1D)
5OA8 · IRON/ALPHA-ketoglutarate-dependent dioxygenase asqj: “FE(II)/(ALPHA)KETOGLUTARATE-dependent dioxygenase ASQJ_V72I mutant in complex with demethylated cyclopeptin…”. X-ray diffraction, 3 ligands (AKG, 58L, NI), 3 pockets (best…
- PDB
- 5OA8
- Type
- protein
- Length
- 288 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- IRON/ALPHA-ketoglutarate-dependent dioxygenase asqj
- EC
- 1.14.-.-
- UniProt
- Q5AR53
- Ligands
- AKG, 58L, NI
- Pockets
- 3 · best druggability 0.73
Structure
x-ray diffraction · 1 distinct chain · 25% helix, 21% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | IRON/ALPHA-ketoglutarate-dependent dioxygenase asqj (EC 1.14.-.-) | protein | 288 | 25% helix, 21% strand | Q5AR53 |
Ligands and binding sites
- AKG · 2-oxoglutaric acid · ligand · chains A
- 58L · demethylated cyclopeptin · ligand · chains A
- NI · Nickel (II) ion · metal · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 423 | 0.73 | 0.83 | 49 | NI, AKG, 58L |
| 2 | 139 | 0.51 | 0.80 | 21 | empty |
| 3 | 56 | 0.31 | 0.75 | 14 | empty |
Compared structures
- 5OA8 · Fe(II)/(alpha)ketoglutarate-dependent dioxygenase AsqJ_V72I mutant in complex with… · the same entry in another collection · chain A against A, TM-score 1.00
- Q5AR53 · AlphaFold monomer V2.0 prediction for IRON/ALPHA-ketoglutarate- dependent dioxygenase… · a predicted model of the same protein · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q5AR53
- Elsewhere: RCSB PDB 5OA8 · PDBe 5OA8 · UniProt Q5AR53
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